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Starting soon Observational

Pain Control and Recovery After Thoracic Surgery Using SPSIP Block

NCT07850388 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-10-01
Last updated
2026-09-30

Condition(s) studied

Postoperative Pain

Investigational drug(s) / intervention(s)

Ultrasound-Guided Serratus Posterior Superior Intercostal Plane Block

Ultrasound-Guided Serratus Posterior Superior Intercostal Plane Block: An ultrasound-guided Serratus Posterior Superior Intercostal Plane (SPSIP) block will be performed after induction of general anesthesia according to routine institutional clinical practice using a long-acting local anesthetic.

Study summary

Thoracic surgery is frequently associated with significant postoperative pain, which may impair respiratory function, mobilization, recovery, and patient satisfaction. The Serratus Posterior Superior Intercostal Plane (SPSIP) block is a recently described ultrasound-guided fascial plane block that may provide effective analgesia after thoracic surgery. This prospective observational cohort study will evaluate the analgesic effectiveness and postoperative recovery associated with SPSIP block in adult patients undergoing elective minor video-assisted thoracoscopic surgery (VATS), major VATS, or thoracotomy. All patients will receive SPSIP block as part of routine institutional multimodal analgesia. The primary outcome will be postoperative quality of recovery assessed using the Quality of Recovery-15 (QoR-15) questionnaire at 24 hours after surgery. Secondary outcomes will include postoperative pain intensity, opioid consumption, rescue analgesic requirements, postoperative nausea and vomiting, pulmonary complications, patient satisfaction, length of hospital stay, and chronic postoperative pain.

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Age 18 years or older * American Society of Anesthesiologists (ASA) physical status I-III * Scheduled for elective thoracic surgery * Undergoing minor video-assisted thoracoscopic surgery (VATS), major VATS, or thoracotomy * Planned ultrasound-guided Serratus Posterior Superior Intercostal Plane (SPSIP) block as part of routine multimodal analgesia * Able and willing to provide written informed consent Exclusion Criteria: * Patient refusal * Known allergy to amide local anesthetics * Coagulopathy * Therapeutic anticoagulation incompatible with regional anesthesia * Infection at the planned block injection site * Pregnancy * Emergency surgery * Chronic opioid therapy for more than 3 months * Chronic pain syndrome * Cognitive impairment that prevents reliable study assessments * Inability to complete the Quality of Recovery-15 (QoR-15) questionnaire

Primary outcome measure(s)

  • Quality of Recovery-15 Score at 24 Hours — 24 hours after surgery
    Postoperative quality of recovery will be assessed using the 15-item Quality of Recovery questionnaire (QoR-15). Higher scores indicate better postoperative recovery. QoR-15 scores will be compared among the minor VATS, major VATS, and thoracotomy cohorts.

Trial sites (1)

FacilityCityRegionStatus
Izmir Katip Celebi University Atatürk Training and Research Hospital, Karabaglar, Izmir Izmir İzmir
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07850388 on ClinicalTrials.gov ↗ ← All trials in Turkey